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EP0403018B1 - Photographische Materialien, die auswaschbare Kuppler enthalten - Google Patents

Photographische Materialien, die auswaschbare Kuppler enthalten Download PDF

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Publication number
EP0403018B1
EP0403018B1 EP90201508A EP90201508A EP0403018B1 EP 0403018 B1 EP0403018 B1 EP 0403018B1 EP 90201508 A EP90201508 A EP 90201508A EP 90201508 A EP90201508 A EP 90201508A EP 0403018 B1 EP0403018 B1 EP 0403018B1
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EP
European Patent Office
Prior art keywords
coupler
photographic element
coup
moiety
group
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EP90201508A
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English (en)
French (fr)
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EP0403018A2 (de
EP0403018A3 (de
Inventor
Gregory James C/O Eastman Kodak Company Lestina
Jon Dolf C/O Eastman Kodak Company Bass
John William C/O Eastman Kodak Company Harder
Stephen Paul C/O Eastman Kodak Company Singer
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Eastman Kodak Co
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Eastman Kodak Co
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Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/32—Colour coupling substances
    • G03C7/3212—Couplers characterised by a group not in coupling site, e.g. ballast group, as far as the coupling rest is not specific
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers

Definitions

  • This invention relates to color photography.
  • it relates to novel dye-forming couplers and to photographic elements containing them.
  • Color photographic images are commonly formed by a reaction between oxidized silver halide developing agent and a dye-forming compound commonly called a coupler. This type of reaction has been used from the time of the earliest commercially viable color photographic materials. Early materials employed a photographic element containing light-sensitive silver halide emulsion layers. The coupler compound was introduced into the element during processing after imagewise exposure. Materials intended for use in this way continue to be sold under the Kodachrome trademark.
  • Such materials provide extremely sharp and stable images.
  • a disadvantage of such materials is the complexity of the development sequence necessitated by the use of couplers in the processing compositions.
  • couplers in the processing compositions.
  • unreacted coupler as an inverse function of dye formation.
  • Such unreacted coupler increases the thickness of the layer in which it remains; hence, it can reduce the sharpness of the image. More significantly, unreacted coupler can deteriorate or undergo side reactions on keeping. This provides a potential for a change in density of the background areas of the image with time.
  • This invention provides novel photographic couplers which accomplish this.
  • a photographic element comprising a support, a silver halide emulsion, and a non-diffusible coupler compound that, during photographic processing, is converted to a form that can be removed from the element if it has not reacted with oxidized silver halide color developing agent
  • the coupler compound has the structure: COUP-LS-BAL wherein:
  • Conversion from the non-diffusible form to the removable form can occur in the development step, although preferably the coupler and processing are designed for it to occur in a subsequent step. Removal can occur in the same processing step as conversion, although it preferably occurs in a separate, subsequent step. Conversion and removal can occur in one of the existing processing steps, but preferably one or both occur in an additional step or steps added to the processing sequence specifically for that purpose.
  • Conversion of the coupler to the removable form can involve reducing the bulk and/or increasing the solubility of the coupler. This can be accomplished by the removal of a ballast group or the unblocking of a solubilizing group or both. This can take place on a portion of the coupler molecule in a non-coupling or coupling position. It is preferable for such reactions to occur at some position on the coupling-off group, i.e., the group which is displaced when the coupler reacts with oxidized developing agent.
  • the product which results from the conversion reaction should remain in the removable form for at least as long as required to be removed from the element. Thereafter, the compound can stay in the converted form, revert to the original form, or go to a new form, depending upon the particular reactions involved.
  • the coupler moiety Upon development, the coupler moiety will react with oxidized color developing agent (DOX). Also, during processing, the linking group splits to detach the ballast from the remainder of the molecule. Various reaction products are possible depending on the particular type of coupler moiety employed, the position on the coupler moiety to which the linking group is attached, and the particular linking group employed.
  • DOX oxidized color developing agent
  • reaction of the coupler compound with oxidized developing agent will yield a reaction product having the structure while splitting of the linking group without reaction with oxidized color developing agent will yield a product having the structure: 2) COUP-LS' where LS' is the residue of the splittable linking group and can be a solubilizing group, or not.
  • the reaction products will have the structures: where the coupler has reacted with oxidized developing agent, and the structure where it has not.
  • COUP and LS′ should be such that products 2 and 4 are removable from the element during processing. This is accomplished by reduction in bulk resulting from cleavage of the ballast group, or by unmasking of a solubilizing group in LS′, or both.
  • COUP is chosen so that products 1 and 3 are non-diffusible image forming dyes.
  • COUP can be chosen so that products 1 or 3 is slightly mobile to result in image smearing as described in US patents 4,420,556 and 4,489,155.
  • the splittable linking group is attached to a non-coupling position of the coupler moiety, there can be attached to the coupling position a group that upon coupling will be released for a photographic effect.
  • the coupling position can be substituted with a non-removable group that will permit a leuco dye to be formed on reaction with oxidized color developing agent, thereby providing a scavenger compound which competes for oxidized color developing agent.
  • COUP it may be advantageous for COUP to be chosen so that product 1 is removed from the element during processing.
  • the coupler moiety represented by COUP can be derived from any of the couplers known in the art which are of suitable bulk and solubility. Preferred are cyan, magenta and yellow dye forming coupler moieties which yield a non-diffusible dye on reaction with oxidized color developing agent, although other coupler moieties can be employed, such as those which yield a colorless or diffusible reaction product with oxidized color developing agent.
  • Couplers which form cyan dyes upon reaction with oxidized color developing agent are described in such representative patents and publications as: U.S. Pat. Nos. 2,772,162; 3,476,563; 4,526,864; 4,500,635; 4,254,212; 4,296,200; 4,457,559; 2,895,826; 3,002,836; 3,034,892; 2,474,293; 2,801,171; 2,423,730; 2,367,531; 3,041,236; 4,443,536; 4,333,999; 4,124,396; 4,775,616; 3,779,763; 3,772,002; 3,419,390; 4,690,889; 3,996,253; and "Farbkuppler-eine Literaturschreibsicht,” published in Agfa Mitanderen, Band III, pp. 156-175 (1961).
  • Such couplers typically are phenols and naphthols.
  • Couplers which form magenta dyes upon reaction with oxidized color developing agent are described in such representative patents and publications as: U.S. Pat. Nos. 2,600,788; 2,369,489; 1,269,479; 2,311,082; 3,061,432; 3,725,067; 4,120,723; 4,500,630; 2,343,703; 2,311,082; 3,152,896; 3,519,429; 3,062,653; 2,908,573; 4,774,172; 4,443,536; 3,935,015, 4,540,654; 4,581,326; European Patent Applications 284,239; 284,240; 240,852; 170,164; 177,765; and "Farbkuppler-eine Literaturubersicht,” published in Agfa Mitanderen, Band III, pp. 126-156 (1961).
  • couplers are pyrazolones, pyrazolotriazoles, pyrazolobenzimidazoles; or indazoles.
  • Couplers which form yellow dyes upon reaction with oxidized and color developing agent are described in such representative patents and publications as: U.S. Pat. Nos. 3,384,657; 3,415,652; 3,542,840; 4,046,575; 3,894,875; 4,095,983; 4,182,630; 2,875,057, 2,407,210, 3,265,506; 2,298,443, 3,408,194; 3,447,928; 4,587,207; 4,617,256; 4,587,205; 4,529,691; 4,443,536; 4,326,024; 4,203,768; 4,221,860; 3,933,501; 4,022,620; 4,401,752; European Patent Application 296,793; and "Farbkuppler-eine Literaturschreibsicht,” published in Agfa Mitanderen, Band III, pp. 112-126 (1961).
  • yellow dye forming couplers are acylacetamides, such as benzoylacetanilides and pivaloylacetanilides.
  • Couplers which form colorless products upon reaction with oxidized color developing agent are described in such representative patents as: U.K. Patent No. 861,138; U.S. Pat. Nos. 3,632,345, 3,928,041; 3,958,993; and 3,961,959.
  • LS In those instances where LS is not joined to the coupling position, there can be attached to the coupling position a photographically useful group, such as a development inhibitor or a development accelerator.
  • a photographically useful group such as a development inhibitor or a development accelerator.
  • Patents describing such couplers include: U.S. Patents 3,148,062; 3,227,554; 4,248,962; 4,409,323; 4,477,563; 4,684,604; 4,737,451; and 4,782,012.
  • the ballast group represented by BAL can be any group of sufficient size and bulk that, with the remainder of the molecule, renders the unreacted coupler immobile prior to processing. It can be a relatively small group if the remainder of the group is relatively bulky. For example, if splitting of LS unmasks a solubilizing group, BAL need not be very bulky if the coupler compound as a whole is non-diffusible. When detached from COUP, the ballast moiety can be mobile and wash out of the element during processing or it can be immobile and remain in the element.
  • ballast moiety is a polymer, from which the coupler moiety is appended, further advantages in the element could be obtained if the polymer eliminated the need for coupler solvent or alternative means of dispersing the coupler in the element. This would have a thinning effect on the entire element which could provide sharpness and image keeping improvements.
  • Splitting of the linking group, LS typically occurs by a hydrolysis reaction which is initiated by a component of one of the processing solutions (e.g. an acid or a base). This reaction can be assisted by a group on the coupler moiety, the ballast group and/or the linking group, or by a group which is a separate component of one of the processing compositions (e.g. a nucleophile).
  • a hydrolysis reaction which is initiated by a component of one of the processing solutions (e.g. an acid or a base).
  • This reaction can be assisted by a group on the coupler moiety, the ballast group and/or the linking group, or by a group which is a separate component of one of the processing compositions (e.g. a nucleophile).
  • Splitting the group LS may leave a solubilizing residue on the coupler.
  • a group can be an acid group, for example a carboxy group.
  • An exemplary reaction is the hydrolysis of an ester.
  • an imidomethyl ester or a beta- or gamma-keto ester can be hydrolyzed in the presence of base and the reaction can be accelerated by the presence of a nucleophile, such as hydroxylamine.
  • a nucleophile such as hydroxylamine.
  • acetal and ketal protecting groups can be hydrolyzed in the presence of acid.
  • hydrolysis is preceded by a separate oxidation or reduction reaction, such as the oxidation of a hydrazide group or of a sulfonamidophenol.
  • the reactions can be anchimerically assisted.
  • Couplers of this invention can be represented by the structure: wherein: COUP is as defined above;
  • the moiety X can complete a mono-, bi- or tri-cyclic ring or ring system each ring of which contains 5 to 6 members.
  • a preferred ring system is the phthalimide (1,3-isoindolinedione) ring system.
  • Other useful ring systems include saccharin, (1,2-benzisothiazolin-3-one-1,1-dioxide), succinimide, maleimide, hydantoin, 2,4-thiazolidinedione, hexahydro-2,4-pyrimidinedione, 1,4-dihydrophthalimide, and the like. These rings can be unsubstituted or substituted.
  • couplers represented by the structures and wherein
  • Suitable substituents include halogen, nitro, alkyl, aryl, alkenyl, alkoxy, aryloxy, alkenyloxy, alkylcarbonyl, arylcarbonyl, alkenylcarbonyl, alkylsulfonyl, arylsulfonyl, alkenylsulfonyl, amino, aminocarbonyl, aminosulfonyl, carboxy, alkoxycarbonyl, aryloxycarbonyl, alkenyloxycarbonyl and the like.
  • alkyl portions of these substituents contain from 1 to about 30 carbon atoms
  • the alkenyl portions of these substituents contain from 2 to about 30 carbon atoms
  • the aryl portions of these substituents contain from 6 to about 30 carbon atoms.
  • the alkyl, aryl and alkenyl portions of these substituents can be further substituted with groups of the type specified above.
  • alkyl is inclusive of, e.g. aralkyl and aryloxyalkyl
  • aryl is inclusive of, e.g., alkaryl and alkoxyaryl.
  • Couplers useful in this invention have the following structures: Couplers useful in this invention can be prepared by sequential stepwise reactions in which there is attached to a preformed coupler moiety the entire -LS-BAL group or the LS group followed by the BAL group. The preparation of representative couplers shown in the following synthesis examples is illustrative of synthetic techniques that can be employed.
  • Part B of Synthesis Example 3 was repeated using 10.2 g (0.02 mole) of Coupler M, 6.2 g (0.01 mole) of disulfide S-8, and 1 g (0.014 mole) of chlorine gas.
  • the couplers of this invention can be incorporated in silver halide emulsions and the emulsions can be coated on a support to form a photographic element.
  • the coupler can be incorporated in the photographic element adjacent to the silver halide emulsion where, during development, the coupler will be in reactive association with development products such as oxidized color developing agent.
  • the photographic elements in which the couplers of this invention are employed can be either single color or multicolor elements.
  • Multicolor elements contain dye image-forming units sensitive to each of the three primary regions of the spectrum.
  • Each unit can be comprised of a single emulsion layer or of multiple emulsion layers sensitive to a given region of the spectrum.
  • the layers of the element, including the layers of the image-forming units, can be arranged in various orders as known in the art.
  • a typical multicolur photographic element comprises a support bearing a cyan dye image-forming unit comprising at least one red-sensitive silver halide emulsion layer having associated therewith at least one cyan dye-forming coupler, a magenta image forming unit comprising at least one green-sensitive silver halide emulsion layer having associated therewith at least one magenta dye-forming coupler and a yellow dye image-forming unit comprising at least one blue-sensitive silver halide emulsion layer having associated therewith at least one yellow dye-forming coupler.
  • the element can contain additional layers, such as filter layers, interlayers, overcoat layers, subbing layers, and the like.
  • the silver halide emulsions employed in the elements of this invention can be comprised of silver bromide, silver chloride, silver iodide, silver chlorobromide, silver chloroiodide, silver bromoiodide, silver chlorobromoiodide or mixtures thereof.
  • the emulsions can include silver halide grains of any conventional shape or size. Specifically, the emulsions can include coarse, medium or fine silver halide grains. High aspect ratio tabular grain emulsions are specifically contemplated, such as those disclosed by Wilgus et al U.S. Patent 4,434,226, Daubendiek et al U.S. Patent 4,414,310, Wey U.S.
  • Patent 4,399,215 Solberg et al U.S. Patent 4,433,048, Mignot U.S. Patent 4,386,156, Evans et al U.S. Patent 4,504,570, Maskasky U.S. Patent 4,400,463, Wey et al U.S. Patent 4,414,306, Maskasky U.S. Patents 4,435,501 and 4,643,966 and Daubendiek et al U.S. Patents 4,672,027 and 4,693,964.
  • Also specifically contemplated are those silver bromoiodide grains with a higher molar proportion of iodide in the core of the grain than in the periphery of the grain, such as those described in U.S.
  • the silver halide emulsions can be either monodisperse or polydisperse as precipitated.
  • the grain size distribution of the emulsions can be controlled by silver halide grain separation techniques or by blending silver halide emulsions of differing grain sizes.
  • Sensitizing compounds such as compounds of copper, thallium, lead, bismuth, cadmium and Group VIII noble metals, can be present during precipitation of the silver halide emulsion.
  • the emulsions can be surface-sensitive emulsions, i.e., emulsions that form latent images primarily on the surfaces of the silver halide grains, or internal latent image-forming emulsions, i.e., emulsions that form latent images predominantly in the interior of the silver halide grains.
  • the emulsions can be negative-working emulsions, such as surface-sensitive emulsions or unfogged internal latent image-forming emulsions, or direct-positive emulsions of the unfogged, internal latent image-forming type, which are positive-working when development is conducted with uniform light exposure or in the presence of a nucleating agent.
  • the silver halide emulsions can be surface sensitized.
  • Noble metal e.g., gold
  • middle chalcogen e.g., sulfur, selenium, or tellurium
  • reduction sensitizers employed individually or in combination, are specifically contemplated.
  • Typical chemical sensitizers are listed in Research Disclosure , Item 17643, cited above, Section III.
  • the silver halide emulsions can be spectrally sensitized with dyes from a variety of classes, including the polymethine dye class, which includes the cyanines, merocyanines, complex cyanines and merocyanines (i.e., tri-, tetra-, and poly-nuclear cyanines and merocyanines), oxonols, hemioxonols, styryls, merostyryls, and streptocyanines.
  • Illustrative spectral sensitizing dyes are disclosed in Research Disclosure , Section IV.
  • Suitable vehicles for the emulsion layers and other layers of elements of this invention are described in Research Disclosure , Section IX and the publications cited therein.
  • the elements of this invention can include additional couplers as described in Research Disclosure , Section VII, paragraphs D, E, F and G and the publications cited therein. These additional couplers can be incorporated as described in Research Disclosure , Section VII, paragraph C and the publications cited therein.
  • the photographic elements of this invention can contain brighteners ( Research Disclosure , Section V), antifoggants and stabilizers ( Research Disclosure , Section VI), antistain agents and image dye stabilizers ( Research Disclosure , Section VII, paragraphs I and J), light absorbing and scattering materials ( Research Disclosure , Section VIII), hardeners ( Research Disclosure , Section X), coating aids ( Research Disclosure , Section XI), plasticizers and lubricants ( Research Disclosure , Section XII), antistatic agents ( Research Disclosure , Section XIII), matting agents ( Research Disclosure , Section XVI) and development modifiers ( Research Disclosure , Section XXI).
  • the photographic elements can be coated on a variety of supports as described in Research Disclosure Section XVII and the references described therein.
  • Photographic elements can be exposed to actinic radiation, typically in the visible region of the spectrum, to form a latent image as described in Research Disclosure Section XVIII and then processed to form a visible dye image as described in Research Disclosure Section XIX.
  • Processing to form a visible dye image includes the step of contacting the element with a color developing agent to reduce developable silver halide and oxidize the color developing agent. Oxidized color developing agent in turn reacts with the coupler to yield a dye.
  • Preferred color developing agents are p-phenylenediamines.
  • 4-amino-3-methyl-N,N-diethylaniline hydrochloride 4-amino-3-methyl-N-ethyl-N- ⁇ -(methanesulfonamido)ethylaniline sulfate hydrate, 4-amino-3-methyl-N-ethyl-N- ⁇ -hydroxyethylaniline sulfate, 4-amino-3- ⁇ -(methanesulfonamido)ethyl-N,N-diethylaniline hydrochloride and 4-amino-N-ethyl-N-(2-methoxyethyl)-m-toluidine di-p-toluenesulfonic acid.
  • this processing step leads to a negative image.
  • this step can be preceded by development with a non-chromogenic developing agent to develop exposed silver halide, but not form dye, and then uniform fogging of the element to render unexposed silver halide developable.
  • a direct positive emulsion can be employed to obtain a positive image.
  • Typical bleach baths contain an oxidizing agent to convert elemental silver, formed during the development step, to silver halide.
  • Suitable bleaching agents include ferricyanides, dichromates, ferric complexes of aminocarboxylic acids and persulfates.
  • Fixing baths contain a complexing agent that will solubilize the silver halide in the element and permit its removal from the element.
  • Typical fixing agents include thiosulfates, bisulfites, and ethylenediamine tetraacetic acid.
  • the bleaching and fixing baths are combined in a bleach/fix bath.
  • the couplers of this invention can be converted to the removable form and removed in one of the processing baths used to perform the conventional functions of development, bleaching, and fixing or bleach/fixing.
  • the removal step and preferably both the conversion and removal steps, be performed in a separate solution.
  • this will be an aqueous alkaline solution, in which the element is placed for a time sufficient to convert and remove coupler which has not reacted to form dye.
  • This step can be between other processing steps, e.g. after development but before bleaching or fixing, but preferably follows bleaching and fixing.
  • a suitable solution comprises an aqueous solution of sodium hydroxide buffered to a pH in the range of 10-13 with a phosphate buffer. Residence times in the solution of several seconds to several minutes, e.g. 30 seconds to 30 minutes may be needed to remove unreacted coupler. The length of time will depend on the composition of the solution, the particular coupler being removed and the amount to be removed.
  • Photographic elements were prepared by coating a gelatin-subbed, polyethylene-coated paper support with a photosensitive layer containing a silver chloride emulsion at 0.172 g Ag/m 2 , gelatin at 1.238 g/m 2 , and one of the magenta couplers as shown in Tables 1-3 at 0.38 mmol/m 2 dispersed in the phosphate ester identified below as A-1 at 50% by weight of coupler. Each coupler dispersion also contained the following addenda (weight percent of coupler): A-2 (32%), A-3 (16%), and ethyl acetate (300%).
  • the photosensitive layer was overcoated with a protective layer containing gelatin at 1.08 g/m 2 and bis(vinylsulfonylmethyl) ether hardener at 2% by weight based on total gelatin.
  • Samples of each element were imagewise exposed through a graduated density test object, then processed at 35°C for 45 seconds in the color developer shown below, 45 seconds in the bleach-fix bath shown below, then washed and dried. Additional samples of each element were exposed and processed as above, except that after the bleach-fix step, the samples were bathed in an aqueous sodium hydroxide bath at pH 11 for 15 minutes.
  • Triethanolamine 11.0 mL Diethylhydroxylamine sulfate (85%) 6.0 mL Lithium sulfate 2.7 g 1-Hydroxyethylene-1,1-diphosphonic acid (60% solution) 0.8 mL 4-Amino-3-methyl-N-ethyl-N-( ⁇ -methanesulfonamido)ethylaniline sulfate hydrate 4.85 g Potassium carbonate 25.0 g Potassium chloride 1.8 g Potassium bromide 0.02 g Stilbene stain-reducing agent 2.3 g Surfactant 0.25 mL Water to make 1.0 L

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Claims (13)

  1. Photographisches Element mit einem Träger, einer Silberhalogenidemulsion sowie einer nicht-diffundierenden Kupplerverbindung, die während der photographischen Entwicklung in eine Form überführt wird, die aus dem Element entfernt werden kann, wenn sie nicht mit oxidierter Silberhalogenidentwicklerverbindung reagiert hat, wobei die Kupplerverbindung die Struktur aufweist:

            COUP-LS-BAL

    worin bedeuten:
    COUP einen Kupplerrest mit einer Kupplungsposition, an der er mit oxidierter Farbentwicklerverbindung zu reagieren vermag,
    LS eine abspaltbare, verbindende Gruppe, die an eine Kupplungs- oder Nicht-Kupplungsposition von COUP gebunden ist, und
    BAL eine Ballastgruppe einer ausreichenden Größe und Sperrigkeit, um die Kupplerverbindung nicht-diffundierend zu machen.
  2. Photographisches Element nach Anspruch 1, in dem der Rest LS-BAL an eine Kupplungsposition von COUP gebunden ist.
  3. Photographisches Element nach Anspruch 1, worin der Rest LS-BAL an eine Nicht-Kupplungsposition von COUP gebunden ist.
  4. Photographisches Element nach einem der Ansprüche 1 - 3, worin COUP für einen Kupplerrest steht, der wenn er mit oxidierter Farbentwicklerverbindung reagiert hat, einen Farbstoff liefert, der in dem photographischen Element nicht diffundiert oder nur schwach diffundiert.
  5. Photographisches Element nach einem der Ansprüche 1 - 4, worin die Abspaltung von LS eine Hydrolysereaktion, eine Oxidationsreaktion, eine Katalysereaktion oder eine Kombination solcher Reaktionen einschließt.
  6. Photographisches Element nach Anspruch 5, worin die Abspaltung von LS eine Hydrolyse eines Esters, eines Ketals oder eines Acetals einschließt.
  7. Photographisches Element nach Anspruch 1, worin die Abspaltung der Gruppe LS an der Kupplerverbindung einen löslichmachenden Rest hinterläßt.
  8. Photographisches Element nach Anspruch 7, worin der löslichmachende Rest eine Säuregruppe ist.
  9. Photographisches Element nach Anspruch 7 oder 8, worin der löslichmachende Rest eine Carboxygruppe ist.
  10. Photographisches Element nach Anspruch 5, worin der Rest LS-BAL an eine Kupplungsposition von COUP gebunden ist und die Struktur aufweist:
    Figure imgb0071
     worin bedeuten:
    Z gleich O oder S oder ein Stickstoffatom eines heterocyclischen Ringes;
    R1 Alkylen mit 1 - 10 Kohlenstoffatomen oder Aryliden mit 6 - 16 Kohlenstoffatomen;
    R2 Wasserstoff, Alkyl mit 1 - 4 Kohlenstoffatomen oder Aryl mit 6 - 12 Kohlenstoffatomen;
    J gleich -CO- oder -SO2-; und
    X die Atome, die zur Vervollständigung eines 5- oder 6-gliedrigen Ringrestes oder Ringsystemrestes erforderlich sind.
  11. Verfahren zur Herstellung eines Bildes in einem photographischen Element nach einem der Ansprüche 1 - 10, das umfaßt die Entwicklung des Elementes unter Bildung eines sichtbaren Bildes und die Entfernung von Kupplerverbindung, die nicht mit oxidierter Farbentwicklerverbindung reagiert hat, aus dem Element.
  12. Verfahren nach Anspruch 11, bei dem die Entfernung der nicht-umgesetzten Kupplerverbindung in einer Stufe erfolgt, die von der Entwicklungsstufe getrennt ist.
  13. Verfahren nach Anspruch 11, bei dem die Entfernung der nicht-umgesetzten Kupplerverbindung in einer Stufe separat von den Entwicklungs-, Bleich- und Fixier- sowie Bleich-/Fixierstufen erfolgt.
EP90201508A 1989-06-16 1990-06-12 Photographische Materialien, die auswaschbare Kuppler enthalten Expired - Lifetime EP0403018B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US07/366,953 US5051343A (en) 1989-06-16 1989-06-16 Photographic elements containing removable couplers
US366953 1994-12-30

Publications (3)

Publication Number Publication Date
EP0403018A2 EP0403018A2 (de) 1990-12-19
EP0403018A3 EP0403018A3 (de) 1991-03-06
EP0403018B1 true EP0403018B1 (de) 1996-09-04

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EP90201508A Expired - Lifetime EP0403018B1 (de) 1989-06-16 1990-06-12 Photographische Materialien, die auswaschbare Kuppler enthalten

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US (1) US5051343A (de)
EP (1) EP0403018B1 (de)
JP (1) JPH0331842A (de)
DE (1) DE69028351T2 (de)

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US5158865A (en) * 1990-12-20 1992-10-27 Eastman Kodak Company Photographic elements containing removable filter dye
US5246820A (en) * 1992-03-03 1993-09-21 Eastman Kodak Company Carbamic acid solubilized smearing couplers
US5296337A (en) * 1992-04-23 1994-03-22 Eastman Kodak Company Process for retouching photographic images containing a dye having a cleavable ballast
US5534401A (en) * 1992-04-23 1996-07-09 Eastman Kodak Company Retouchable reversal silver halide photographic element with a pyrazoloazole magenta dye-forming coupler
EP0574090A1 (de) 1992-06-12 1993-12-15 Eastman Kodak Company 1-Äquivalentkuppler und freisetzbaren Farbstoffen mit niedrigem pKa
US5424179A (en) * 1994-08-11 1995-06-13 Eastman Kodak Company Photographic element with a cyclic azole coupler having a saccharin substituent

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Also Published As

Publication number Publication date
DE69028351D1 (de) 1996-10-10
US5051343A (en) 1991-09-24
DE69028351T2 (de) 1997-04-10
JPH0331842A (ja) 1991-02-12
EP0403018A2 (de) 1990-12-19
EP0403018A3 (de) 1991-03-06

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